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Onion peel extract and its constituent, quercetin inhibits human Slo3 in a pH and calcium dependent manner

Sperm function and male fertility are closely related to pH dependent K(+) current (KSper) in human sperm, which is most likely composed of Slo3 and its auxiliary subunit leucine-rich repeat-containing protein 52 (LRRC52). Onion peel extract (OPE) and its major active ingredient quercetin are widely...

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Autores principales: Wijerathne, Tharaka Darshana, Kim, Ji Hyun, Kim, Min Ji, Kim, Chul Young, Chae, Mee Ree, Lee, Sung Won, Lee, Kyu Pil
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Physiological Society and The Korean Society of Pharmacology 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6717788/
https://www.ncbi.nlm.nih.gov/pubmed/31496875
http://dx.doi.org/10.4196/kjpp.2019.23.5.381
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author Wijerathne, Tharaka Darshana
Kim, Ji Hyun
Kim, Min Ji
Kim, Chul Young
Chae, Mee Ree
Lee, Sung Won
Lee, Kyu Pil
author_facet Wijerathne, Tharaka Darshana
Kim, Ji Hyun
Kim, Min Ji
Kim, Chul Young
Chae, Mee Ree
Lee, Sung Won
Lee, Kyu Pil
author_sort Wijerathne, Tharaka Darshana
collection PubMed
description Sperm function and male fertility are closely related to pH dependent K(+) current (KSper) in human sperm, which is most likely composed of Slo3 and its auxiliary subunit leucine-rich repeat-containing protein 52 (LRRC52). Onion peel extract (OPE) and its major active ingredient quercetin are widely used as fertility enhancers; however, the effect of OPE and quercetin on Slo3 has not been elucidated. The purpose of this study is to investigate the effect of quercetin on human Slo3 channels. Human Slo3 and LRRC52 were co-transfected into HEK293 cells and pharmacological properties were studied with the whole cell patch clamp technique. We successfully expressed and measured pH sensitive and calcium insensitive Slo3 currents in HEK293 cells. We found that OPE and its key ingredient quercetin inhibit Slo3 currents. Inhibition by quercetin is dose dependent and this degree of inhibition decreases with elevating internal alkalization and internal free calcium concentrations. Functional moieties in the quercetin polyphenolic ring govern the degree of inhibition of Slo3 by quercetin, and the composition of such functional moieties are sensitive to the pH of the medium. These results suggest that quercetin inhibits Slo3 in a pH and calcium dependent manner. Therefore, we surmise that quercetin induced depolarization in spermatozoa may enhance the voltage gated proton channel (Hv1), and activate non-selective cation channels of sperm (CatSper) dependent calcium influx to trigger sperm capacitation and acrosome reaction.
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spelling pubmed-67177882019-09-06 Onion peel extract and its constituent, quercetin inhibits human Slo3 in a pH and calcium dependent manner Wijerathne, Tharaka Darshana Kim, Ji Hyun Kim, Min Ji Kim, Chul Young Chae, Mee Ree Lee, Sung Won Lee, Kyu Pil Korean J Physiol Pharmacol Original Article Sperm function and male fertility are closely related to pH dependent K(+) current (KSper) in human sperm, which is most likely composed of Slo3 and its auxiliary subunit leucine-rich repeat-containing protein 52 (LRRC52). Onion peel extract (OPE) and its major active ingredient quercetin are widely used as fertility enhancers; however, the effect of OPE and quercetin on Slo3 has not been elucidated. The purpose of this study is to investigate the effect of quercetin on human Slo3 channels. Human Slo3 and LRRC52 were co-transfected into HEK293 cells and pharmacological properties were studied with the whole cell patch clamp technique. We successfully expressed and measured pH sensitive and calcium insensitive Slo3 currents in HEK293 cells. We found that OPE and its key ingredient quercetin inhibit Slo3 currents. Inhibition by quercetin is dose dependent and this degree of inhibition decreases with elevating internal alkalization and internal free calcium concentrations. Functional moieties in the quercetin polyphenolic ring govern the degree of inhibition of Slo3 by quercetin, and the composition of such functional moieties are sensitive to the pH of the medium. These results suggest that quercetin inhibits Slo3 in a pH and calcium dependent manner. Therefore, we surmise that quercetin induced depolarization in spermatozoa may enhance the voltage gated proton channel (Hv1), and activate non-selective cation channels of sperm (CatSper) dependent calcium influx to trigger sperm capacitation and acrosome reaction. The Korean Physiological Society and The Korean Society of Pharmacology 2019-09 2019-08-26 /pmc/articles/PMC6717788/ /pubmed/31496875 http://dx.doi.org/10.4196/kjpp.2019.23.5.381 Text en Copyright © Korean J Physiol Pharmacol http://creativecommons.org/licenses/by-nc/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Wijerathne, Tharaka Darshana
Kim, Ji Hyun
Kim, Min Ji
Kim, Chul Young
Chae, Mee Ree
Lee, Sung Won
Lee, Kyu Pil
Onion peel extract and its constituent, quercetin inhibits human Slo3 in a pH and calcium dependent manner
title Onion peel extract and its constituent, quercetin inhibits human Slo3 in a pH and calcium dependent manner
title_full Onion peel extract and its constituent, quercetin inhibits human Slo3 in a pH and calcium dependent manner
title_fullStr Onion peel extract and its constituent, quercetin inhibits human Slo3 in a pH and calcium dependent manner
title_full_unstemmed Onion peel extract and its constituent, quercetin inhibits human Slo3 in a pH and calcium dependent manner
title_short Onion peel extract and its constituent, quercetin inhibits human Slo3 in a pH and calcium dependent manner
title_sort onion peel extract and its constituent, quercetin inhibits human slo3 in a ph and calcium dependent manner
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6717788/
https://www.ncbi.nlm.nih.gov/pubmed/31496875
http://dx.doi.org/10.4196/kjpp.2019.23.5.381
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